A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742541



Internal ID20518525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62332122..62332559hg38UCSC Ensembl
chr15:62624321..62624758hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742541
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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